RecallHawk

RUFINAMIDE

CHARTWELL RX

Summary

FDA approved RUFINAMIDE by CHARTWELL RX. ANDA (Generic) approval on 2022-11-07. SUSPENSION, ORAL.

Details

Source

Drug Approval

External ID

ANDA214009-1

Action Date

2022-11-07

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

RUFINAMIDE, SUSPENSION, ORAL. Application: ANDA214009

Context & Analysis

CHARTWELL RX has 64 FDA actions in our database.

Frequently Asked Questions

How often does CHARTWELL RX have FDA actions?

CHARTWELL RX has 64 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA214009-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for drug

Related Actions